Matches in Nanopublications for { ?s ?p "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.